Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2302
Gene Symbol: FOXJ1
FOXJ1
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.510 GermlineCausalMutation ORPHANET De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry. 31630787

2019